Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs229662261
- Species
- Mus musculus
- Symbol
- rs229662261
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Lhx9
- Location
- 1:138762089
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000067.7:g.138762089A>C
- HGVS.c name
- ENSEMBL:ENSMUST00000019374.1:c.734-1447T>G
- ENSEMBL:ENSMUST00000046870.1:c.707-1447T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:138752924...138776315 (23.39 kb)
- Assembly version
- Not Available
- Viewer Help
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